Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry

被引：0
|
作者：
Helen E. Jo
Ian Glaspole
Yuben Moodley
Sally Chapman
Samantha Ellis
Nicole Goh
Peter Hopkins
Greg Keir
Annabelle Mahar
Wendy Cooper
Paul Reynolds
E. Haydn Walters
Christopher Zappala
Christopher Grainge
Heather Allan
Sacha Macansh
Tamera J. Corte
机构：
[1] Royal Prince Alfred Hospital,School of Medicine
[2] University of Sydney,School of Medicine
[3] The Alfred Hospital,undefined
[4] Fiona Stanley Hospital,undefined
[5] Royal Adelaide Hospital,undefined
[6] The Austin Hospital,undefined
[7] Prince Charles Hospital,undefined
[8] Princess Alexandria Hospital,undefined
[9] Western Sydney University,undefined
[10] University of Tasmania,undefined
[11] University of Tasmania,undefined
[12] Royal Brisbane and Women’s Hospital,undefined
[13] John Hunter Hospital,undefined
[14] Lung Foundation Australia,undefined
来源：
BMC Pulmonary Medicine | / 18卷
关键词：
Idiopathic pulmonary fibrosis; Interstitial lung disease; Disease severity;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [21] QUALITY OF LIFE OF PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS (IPF)-WHAT CAN THE AUSTRALIAN IPF REGISTRY TELL US?
    Glaspole, I
    Goh, N.
    Hopkins, P.
    Moodley, Y.
    Reynolds, P.
    Walters, H.
    Wood-Baker, R.
    Zappala, C.
    Chapman, S.
    Cooper, W.
    Darbishire, W.
    Ellis, S.
    Mahar, A.
    Macansh, S.
    Corte, T.
    Chaplin, H.
    Fuller, J.
    Mcalister, M.
    Stevens, E.
    Smith, S.
    RESPIROLOGY, 2014, 19 : 94 - 94
  • [22] Quality Of Life Of Patients With Idiopathic Pulmonary Fibrosis (ipf) - What Can The Australian Ipf Registry Tell Us?
    Glaspole, I.
    Goh, N.
    Hopkins, P.
    Moodley, Y.
    Reynolds, P. N.
    Walters, H.
    Wood-Baker, R.
    Zappala, C.
    Chapman, S.
    Cooper, W.
    Darbishire, W.
    Ellis, S.
    Mahar, A.
    Chaplin, H.
    Fuller, J.
    Macansh, S.
    McAlister, M.
    Stevens, E.
    Smith, S.
    Symons, K.
    Webster, S.
    Corte, T.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 189
  • [23] Pirfenidone Is Efficacious In Patients With Idiopathic Pulmonary Fibrosis (ipf) And Mild Restrictive Disease
    Albera, C.
    Bradford, W. Z.
    Costabel, U.
    Fagan, E. A.
    Glaspole, I.
    Glassberg, M. K.
    Gorina, E.
    Kardatzke, D.
    King, T. E.
    Lancaster, L.
    Lederer, D. J.
    Nathan, S. D.
    Pereira, C.
    Spirig, D.
    Swigris, J. J.
    Valeyre, D.
    Noble, P. W.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191
  • [24] Survival in Patients with Idiopathic Pulmonary Fibrosis (IPF): Data from the IPF-PRO Registry
    Palmer, S. M.
    Snyder, L.
    Neely, M. L.
    Yow, E.
    Bender, S.
    Culver, D. A.
    de Andrade, J.
    Gulati, M.
    Kaner, R. J.
    Leonard, T.
    O'Brien, E.
    Pushlar, N.
    Conoscenti, C. S.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 197
  • [25] Implications of the diagnostic criteria of idiopathic pulmonary fibrosis in clinical practice: Analysis from the Australian Idiopathic Pulmonary Fibrosis Registry
    Jo, Helen E.
    Glaspole, Ian
    Goh, Nicole
    Hopkins, Peter M. A.
    Moodley, Yuben
    Reynolds, Paul N.
    Chapman, Sally
    Walters, Eugene Haydn
    Zappala, Christopher
    Allan, Heather
    Macansh, Sacha
    Grainge, Christopher
    Keir, Gregory J.
    Hayen, Andrew
    Henderson, Douglas
    Klebe, Sonja
    Heinze, Stefan B.
    Miller, Anne
    Rouse, Hannah C.
    Duhig, Edwina
    Cooper, Wendy A.
    Mahar, Annabelle M.
    Ellis, Samantha
    McCormack, Samuel R.
    Ng, Bernard
    Godbolt, David B.
    Corte, Tamera J.
    RESPIROLOGY, 2019, 24 (04) : 361 - 368
  • [26] Disease progression in idiopathic pulmonary fibrosis without pulmonary function impairment
    Kondoh, Yasuhiro
    Taniguchi, Hiroyuki
    Ogura, Takashi
    Johkoh, Takeshi
    Fujimoto, Kiminori
    Sumikawa, Hiromitsu
    Kataoka, Kensuke
    Baba, Tomohisa
    Colby, Thomas V.
    Kitaichi, Masanori
    RESPIROLOGY, 2013, 18 (05) : 820 - 826
  • [27] Multidisciplinary Review Of Idiopathic Pulmonary Fibrosis (ipf) Patients: Review Of Clinical Diagnosis For Patients Referred To The Australian Ipf Registry
    Glaspole, I.
    Goh, N.
    Hopkins, P.
    Moodley, Y.
    Reynolds, P. N.
    Walters, E.
    Zappala, C.
    Allan, H.
    Chapman, S.
    Cooper, W.
    Ellis, S.
    Grainge, C.
    Jo, H.
    Keir, G.
    Mahar, A.
    Chaplin, H.
    Fuller, J.
    Henson, R.
    Macansh, S.
    Richards, S.
    Symons, K.
    Corte, T. J.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191
  • [28] MULTIDISCIPLINARY REVIEW OF IDIOPATHIC PULMONARY FIBROSIS (IPF) PATIENTS: REVIEW OF CLINICAL DIAGNOSIS FOR PATIENTS REFERRED TO THE AUSTRALIAN IPF REGISTRY
    Glaspole, I
    Goh, N.
    Hopkins, P.
    Moodley, Y.
    Reynolds, P.
    Walters, E.
    Zappala, C.
    Allan, H.
    Chapman, S.
    Cooper, W.
    Ellis, S.
    Grainge, C.
    Jo, H.
    Keir, G.
    Mahar, A.
    Chaplin, H.
    Fuller, J.
    Henson, R.
    Macansh, S.
    Richards, S.
    Symons, K.
    Corte, T. J.
    RESPIROLOGY, 2015, 20 : 59 - 59
  • [29] Baseline characteristics of idiopathic pulmonary fibrosis: analysis from the Australian Idiopathic Pulmonary Fibrosis Registry (vol 49, 1601592, 2017)
    Jo, Helen E.
    Glaspole, Ian
    Grainge, Christopher
    Goh, Nicole
    Hopkins, Peter M. A.
    Moodley, Yuben
    Reynolds, Paul N.
    Chapman, Sally
    Walters, E. Haydn
    Zappala, Christopher
    Allan, Heather
    Keir, Gregory J.
    Hayen, Andrew
    Cooper, Wendy A.
    Mahar, Annabelle M.
    Ellis, Samantha
    Macansh, Sacha
    Corte, Tamera J.
    EUROPEAN RESPIRATORY JOURNAL, 2017, 49 (03)
  • [30] HOSPITALIZATIONS AND OUTCOMES IN PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS (IPF): INSIGHTS FROM THE IPF-PRO REGISTRY
    Kim, Hyun
    Neely, Megan
    Janssen, Katherine
    Adegunsoye, Ayodeji
    Strek, Mary
    Yow, Eric
    Conoscenti, Craig
    Leonard, Thomas
    Snyder, Laurie
    CHEST, 2020, 158 (04) : 1062A - 1063A
12345